PhenomeGene — Human Disease Gene Website SeriesTENM3

TENM3

This website provides information on patients with mutations in the TENM3gene, including clinical data, molecular data, management and research options.

The syndrome caused by mutations in the TENM3gene is a multisystem disorder characterized by ocular and neurodevelopmental features.

Not all individuals with a mutation in the TENM3gene have these features.

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the TENM3gene.

Nicolas Chassaing, MD, PhD, Clinical and Biological French Reference Center for genetic ocular malformations in Toulouse University Hospital, Toulouse, France, chassaing.n@chu-toulouse.fr
Julie Plaisancié, MD, PhD, Clinical and Biological French Reference Center for genetic ocular malformations in Toulouse University Hospital, Toulouse, France, plaisancie.j@chu-toulouse.fr